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Items: 1 to 20 of 60

1.

Validation of the Child HCAHPS survey to measure pediatric inpatient experience of care in Flanders.

Bruyneel L, Coeckelberghs E, Buyse G, Casteels K, Lommers B, Vandersmissen J, Van Eldere J, Van Geet C, Vanhaecht K.

Eur J Pediatr. 2017 Jul;176(7):935-945. doi: 10.1007/s00431-017-2919-7. Epub 2017 May 24.

PMID:
28540435
2.

Long-Term Efficacy, Safety, and Pharmacokinetics of Drisapersen in Duchenne Muscular Dystrophy: Results from an Open-Label Extension Study.

Goemans NM, Tulinius M, van den Hauwe M, Kroksmark AK, Buyse G, Wilson RJ, van Deutekom JC, de Kimpe SJ, Lourbakos A, Campion G.

PLoS One. 2016 Sep 2;11(9):e0161955. doi: 10.1371/journal.pone.0161955. eCollection 2016.

3.

Differences in Contraction-Induced Hemodynamics and Surface EMG in Duchenne Muscular Dystrophy.

Van Ginderdeuren E, Caicedo A, Taelmans J, Goemans N, van den Hauwe M, Naulaers G, Van Huffel S, Buyse G.

Adv Exp Med Biol. 2016;876:71-77. doi: 10.1007/978-1-4939-3023-4_9.

PMID:
26782197
4.

Investigating the genetic basis of fever-associated syndromic epilepsies using copy number variation analysis.

Hartmann C, von Spiczak S, Suls A, Weckhuysen S, Buyse G, Vilain C, Van Bogaert P, De Jonghe P, Cook J, Muhle H, Stephani U, Helbig I, Mefford HC.

Epilepsia. 2015 Mar;56(3):e26-32. doi: 10.1111/epi.12920. Epub 2015 Feb 17.

5.

Current treatment and management of dystrophinopathies.

Goemans N, Buyse G.

Curr Treat Options Neurol. 2014 May;16(5):287. doi: 10.1007/s11940-014-0287-4.

PMID:
24619767
6.

Long-term outcome of intravesical oxybutynin in children with detrusor-sphincter dyssynergia: with special reference to age-dependent parameters.

Humblet M, Verpoorten C, Christiaens MH, Hirche H, Jansen K, Buyse G, van Gool JD.

Neurourol Urodyn. 2015 Apr;34(4):336-42. doi: 10.1002/nau.22560. Epub 2014 Jan 16.

PMID:
24436114
7.

Six-minute walk test: reference values and prediction equation in healthy boys aged 5 to 12 years.

Goemans N, Klingels K, van den Hauwe M, Boons S, Verstraete L, Peeters C, Feys H, Buyse G.

PLoS One. 2013 Dec 31;8(12):e84120. doi: 10.1371/journal.pone.0084120. eCollection 2013.

8.

PRRT2 mutations: exploring the phenotypical boundaries.

Djémié T, Weckhuysen S, Holmgren P, Hardies K, Van Dyck T, Hendrickx R, Schoonjans AS, Van Paesschen W, Jansen AC, De Meirleir L, Selim LA, Girgis MY, Buyse G, Lagae L, Smets K, Smouts I, Claeys KG, Van den Bergh V, Grisar T, Blatt I, Shorer Z, Roelens F, Afawi Z, Helbig I, Ceulemans B, De Jonghe P, Suls A.

J Neurol Neurosurg Psychiatry. 2014 Apr;85(4):462-5. doi: 10.1136/jnnp-2013-305122. Epub 2013 Oct 7.

PMID:
24101679
9.

Ambulatory capacity and disease progression as measured by the 6-minute-walk-distance in Duchenne muscular dystrophy subjects on daily corticosteroids.

Goemans N, van den Hauwe M, Wilson R, van Impe A, Klingels K, Buyse G.

Neuromuscul Disord. 2013 Aug;23(8):618-23. doi: 10.1016/j.nmd.2013.05.006. Epub 2013 Jun 13.

PMID:
23770101
10.

Functional studies and proteomics in platelets and fibroblasts reveal a lysosomal defect with increased cathepsin-dependent apoptosis in ATP1A3 defective alternating hemiplegia of childhood.

Di Michele M, Goubau C, Waelkens E, Thys C, De Vos R, Overbergh L, Schyns T, Buyse G, Casaer P, Van Geet C, Freson K.

J Proteomics. 2013 Jun 28;86:53-69. doi: 10.1016/j.jprot.2013.05.005. Epub 2013 May 13.

PMID:
23681173
11.

Platelet defects in congenital variant of Rett syndrome patients with FOXG1 mutations or reduced expression due to a position effect at 14q12.

Goubau C, Devriendt K, Van der Aa N, Crepel A, Wieczorek D, Kleefstra T, Willemsen MH, Rauch A, Tzschach A, de Ravel T, Leemans P, Van Geet C, Buyse G, Freson K.

Eur J Hum Genet. 2013 Dec;21(12):1349-55. doi: 10.1038/ejhg.2013.86. Epub 2013 May 1.

12.

Test-retest reliability and developmental evolution of the 6-min walk test in Caucasian boys aged 5-12 years.

Goemans N, Klingels K, van den Hauwe M, Van Orshoven A, Vanpraet S, Feys H, Buyse G.

Neuromuscul Disord. 2013 Jan;23(1):19-24. doi: 10.1016/j.nmd.2012.10.019. Epub 2012 Nov 6.

PMID:
23137525
13.

Chiasmal optic neuritis in a 4-year-old girl: a case report and review of the literature.

Caluwaerts E, De Waele L, Buyse G, Demaerel P, Casteels I.

Bull Soc Belge Ophtalmol. 2012;(320):5-10. Review.

PMID:
22978178
14.

Ring chromosome 20 syndrome: electroclinical description of six patients and review of the literature.

Elens I, Vanrykel K, De Waele L, Jansen K, Segeren M, Van Paesschen W, Ceulemans B, Boel M, Frijns JP, Buyse G, Lagae L.

Epilepsy Behav. 2012 Apr;23(4):409-14. doi: 10.1016/j.yebeh.2012.02.008. Epub 2012 Mar 15. Review.

PMID:
22424860
15.

Systemic administration of PRO051 in Duchenne's muscular dystrophy.

Goemans NM, Tulinius M, van den Akker JT, Burm BE, Ekhart PF, Heuvelmans N, Holling T, Janson AA, Platenburg GJ, Sipkens JA, Sitsen JM, Aartsma-Rus A, van Ommen GJ, Buyse G, Darin N, Verschuuren JJ, Campion GV, de Kimpe SJ, van Deutekom JC.

N Engl J Med. 2011 Apr 21;364(16):1513-22. doi: 10.1056/NEJMoa1011367. Epub 2011 Mar 23. Erratum in: N Engl J Med. 2011 Oct 6;365(14):1361.

16.

Neuromyelitis optica-IgG+ optic neuritis associated with celiac disease and dysgammaglobulinemia: a role for tacrolimus?

Meyts I, Jansen K, Renard M, Bossuyt X, Roelens F, Régal L, Lagae L, Buyse G.

Eur J Paediatr Neurol. 2011 May;15(3):265-7. doi: 10.1016/j.ejpn.2010.09.005. Epub 2010 Nov 12.

PMID:
20937563
17.

Treatment of a giant basilar artery aneurysm with a bridging stent and subsequent coil occlusion of the stent: case report.

Wilms G, Buyse G, van Loon J, Maleux G.

Neurosurgery. 2010 Aug;67(2):E510-1. doi: 10.1227/01.NEU.0000372225.37968.29.

PMID:
20644381
18.

Congenital anterolateral bowing of the tibia with ipsilateral polydactyly of the great toe associated with cerebral cyst: a new entity?

Breckpot J, Thienpont B, Vanhole C, Van Rossem E, Van Schoubroeck D, Fryns JP, Lagae L, Buyse G, Devriendt K.

Clin Dysmorphol. 2009 Oct;18(4):195-200. doi: 10.1097/MCD.0b013e32832d06d7.

PMID:
19617820
19.

Idebenone: an emerging therapy for Friedreich ataxia.

Meier T, Buyse G.

J Neurol. 2009 Mar;256 Suppl 1:25-30. doi: 10.1007/s00415-009-1005-0. Review.

PMID:
19283347
20.

Refinement of cortical dysgeneses spectrum associated with TUBA1A mutations.

Bahi-Buisson N, Poirier K, Boddaert N, Saillour Y, Castelnau L, Philip N, Buyse G, Villard L, Joriot S, Marret S, Bourgeois M, Van Esch H, Lagae L, Amiel J, Hertz-Pannier L, Roubertie A, Rivier F, Pinard JM, Beldjord C, Chelly J.

J Med Genet. 2008 Oct;45(10):647-53. doi: 10.1136/jmg.2008.058073. Epub 2008 Aug 26.

PMID:
18728072

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